REGIOSELECTIVE SYNTHESIS AND ANTIMICROBIAL ACTIVITY OF O-ALKYLATED PHYSCION'S DERIVATIVES
Regioselectivity in the reaction of microwave promoted O-alkylation of physcion in the presence of montmorillonite clay K-10 was discussed. The mechanism of formation of corresponding anions of physcion was investigated using semiempirical molecular-orbital methods. The results of antibacterial and...
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Sociedad Chilena de Química
2007
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oai:scielo:S0717-970720070004000142008-04-30REGIOSELECTIVE SYNTHESIS AND ANTIMICROBIAL ACTIVITY OF O-ALKYLATED PHYSCION'S DERIVATIVESMANOJLOVIC,NMARKOVIC,ZDURIC,M physcion O-alkylation regio selective synthesis antimicrobial activity Regioselectivity in the reaction of microwave promoted O-alkylation of physcion in the presence of montmorillonite clay K-10 was discussed. The mechanism of formation of corresponding anions of physcion was investigated using semiempirical molecular-orbital methods. The results of antibacterial and antifungal activity of the obtained derivatives showed that the introduction of different substituents (OCF£3, OCH2C(CH3)=CH2, OCH2CH2CH3 and OCH2C6H5), at the C-1 and C-8 atoms led to a remarkable change in their antimicrobial activityinfo:eu-repo/semantics/openAccessSociedad Chilena de QuímicaJournal of the Chilean Chemical Society v.52 n.4 20072007-01-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072007000400014en10.4067/S0717-97072007000400014 |
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Scielo Chile |
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Scielo Chile |
language |
English |
topic |
physcion O-alkylation regio selective synthesis antimicrobial activity |
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physcion O-alkylation regio selective synthesis antimicrobial activity MANOJLOVIC,N MARKOVIC,Z DURIC,M REGIOSELECTIVE SYNTHESIS AND ANTIMICROBIAL ACTIVITY OF O-ALKYLATED PHYSCION'S DERIVATIVES |
description |
Regioselectivity in the reaction of microwave promoted O-alkylation of physcion in the presence of montmorillonite clay K-10 was discussed. The mechanism of formation of corresponding anions of physcion was investigated using semiempirical molecular-orbital methods. The results of antibacterial and antifungal activity of the obtained derivatives showed that the introduction of different substituents (OCF£3, OCH2C(CH3)=CH2, OCH2CH2CH3 and OCH2C6H5), at the C-1 and C-8 atoms led to a remarkable change in their antimicrobial activity |
author |
MANOJLOVIC,N MARKOVIC,Z DURIC,M |
author_facet |
MANOJLOVIC,N MARKOVIC,Z DURIC,M |
author_sort |
MANOJLOVIC,N |
title |
REGIOSELECTIVE SYNTHESIS AND ANTIMICROBIAL ACTIVITY OF O-ALKYLATED PHYSCION'S DERIVATIVES |
title_short |
REGIOSELECTIVE SYNTHESIS AND ANTIMICROBIAL ACTIVITY OF O-ALKYLATED PHYSCION'S DERIVATIVES |
title_full |
REGIOSELECTIVE SYNTHESIS AND ANTIMICROBIAL ACTIVITY OF O-ALKYLATED PHYSCION'S DERIVATIVES |
title_fullStr |
REGIOSELECTIVE SYNTHESIS AND ANTIMICROBIAL ACTIVITY OF O-ALKYLATED PHYSCION'S DERIVATIVES |
title_full_unstemmed |
REGIOSELECTIVE SYNTHESIS AND ANTIMICROBIAL ACTIVITY OF O-ALKYLATED PHYSCION'S DERIVATIVES |
title_sort |
regioselective synthesis and antimicrobial activity of o-alkylated physcion's derivatives |
publisher |
Sociedad Chilena de Química |
publishDate |
2007 |
url |
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072007000400014 |
work_keys_str_mv |
AT manojlovicn regioselectivesynthesisandantimicrobialactivityofoalkylatedphyscionsderivatives AT markovicz regioselectivesynthesisandantimicrobialactivityofoalkylatedphyscionsderivatives AT duricm regioselectivesynthesisandantimicrobialactivityofoalkylatedphyscionsderivatives |
_version_ |
1718445379846930432 |